Pregled bibliografske jedinice broj: 604113
JAK2-V617F mutation is associated with clinical and laboratory features of myeloproliferative neoplasms
JAK2-V617F mutation is associated with clinical and laboratory features of myeloproliferative neoplasms // Collegium antropologicum, 36 (2012), 3; 859-865 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 604113 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
JAK2-V617F mutation is associated with clinical and laboratory features of myeloproliferative neoplasms
Autori
Naćinović Duletić, Antica ; Dekanić, Andrea ; Hadžisejdić, Ita ; Kušen, Ivona ; Matušan-Ilijaš, Koviljka ; Grohovac, Dragana ; Grahovac, Blaženka ; Jonjić, Nives
Izvornik
Collegium antropologicum (0350-6134) 36
(2012), 3;
859-865
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
JAK2-V617F; essential thrombocythemia; polycythemia vera; primary myelofibrosis
(JAK2-V617F; essential thrombocythemia; polycythemia vera; primary myelofibrosis.)
Sažetak
The aim of this study is to investigate the differences of clinical and laboratory parameters between patients with JAK2-V617F positive myeloproliferative neoplasms (MPNs) and JAK2 wild type MPNs. DNA was isolated from peripheral blood granulocytes of 106 patients treated at Rijeka University Hospital Center: 41 with polycythemia vera (PV), 43 with essential thrombocythemia (ET), 9 with primary myelofibrosis (PMF) and 13 with myeloproliferative neoplasm- -unclassifiable (MPN-u). The JAK2-V617F mutation was detected using allele specific PCR. Laboratory and clinical parameters were obtained from patient’s medical records. The JAK2-V617F mutation was detected in 69% (73/106) patients with MPNs. The results revealed significantly different prevalence of JAK2-V617F mutation, between MPNs entities: 88% in PV, 58% in ET, 56% in PMF and 54% in MPNs-unclassified disorders. The JAK2-V617F mutation significantly correlated with higher leukocyte count and alkaline phosphatase score in ET group and with higher platelets count, leukocyte alkaline phosphatase score and serum lactate dehydrogenase in PV group. Vascular events were associated with elevated platelets count in wholeMPNs group, with higher platelets and leukocyte count in ET and with splenomegaly in PV patients. Clinical and laboratory data revealed significant contribution of JAK2-V617F mutation to the development of clinical phenotype in patients with distinct subgroups of MPNs.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
062-0620095-0082 - REGULACIJSKI ČIMBENICI ANGIOGENEZE U PROGNOZI TUMORA (Jonjić, Nives, MZOS ) ( CroRIS)
062-1081872-0091 - Angiogeneza u agresivnih ne-Hodgkinovih limfoma (Duletić-Načinović, Antica, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka
Profili:
Nives Jonjić
(autor)
Ita Hadžisejdić
(autor)
Andrea Dekanić
(autor)
Dragana Grohovac
(autor)
Blaženka Grahovac
(autor)
Koviljka Matušan Ilijaš
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Social Science Citation Index (SSCI)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE